WormBase Tree Display for Variation: WBVar01767742

WBVar01767742 Name: Public_name: WBVar01767742
    Other_name: cewivar00467970
      H10E21.3b.1:c.798A>G
      CE28733:p.Leu248=
      H10E21.3a.1:c.744A>G
      CE19488:p.Leu266=
    HGVSg: CHROMOSOME_III:g.13317T>C
  Sequence_details: SMap: S_parent: Sequence: H10E21
    Flanking_sequences: CTCGGGCCAGGTTTGGAGCCACTCGTAGAC AGCATTATGTGTGTTTTTATGGTTAGACGA
    Mapping_target: H10E21
    Source_location: 225 CHROMOSOME_III 13317 13317 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00003670
    Transcript: H10E21.3b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3b.1:c.798A>G
        HGVSp: CE19488:p.Leu266=
        cDNA_position: 798
        CDS_position: 798
        Protein_position: 266
        Exon_number: 4/7
        Codon_change: ctA/ctG
        Amino_acid_change: L
      H10E21.3a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3a.1:c.744A>G
        HGVSp: CE28733:p.Leu248=
        cDNA_position: 860
        CDS_position: 744
        Protein_position: 248
        Exon_number: 6/9
        Codon_change: ctA/ctG
        Amino_acid_change: L
  Method: WGS_Flibotte